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NCT Number: NCT07580196

Bilateral Versus Unilateral Lymph Node Dissection in High-Risk Prostate Cancer (BALANCE)

BALANCE is a multicenter, prospective, randomized controlled trial enrolling men with unilateral high-risk localized prostate cancer identified by prostate biopsy, multiparametric MRI, and PSMA PET imaging. Eligible patients scheduled for robot-assisted radical prostatectomy will be randomized in a 1:1 ratio to undergo either unilateral extended pelvic lymph node dissection or bilateral extended pelvic lymph node dissection.

Pelvic lymph node dissection is commonly performed in high-risk prostate cancer for staging purposes, but its therapeutic benefit remains uncertain and the procedure may increase operative time, costs, and postoperative morbidity. Modern imaging techniques may improve the identification of patients with predominantly unilateral disease and support a more selective surgical approach.

The co-primary objectives are to compare 3-year biochemical recurrence-free survival and early postoperative PSA persistence between the two surgical strategies. Secondary objectives include comparison of perioperative complications, operative time, blood loss, length of hospital stay, quality of life, long-term oncologic outcomes, and costs.

This study is designed to determine whether unilateral extended pelvic lymph node dissection can reduce surgical morbidity while preserving oncologic outcomes in appropriately selected patients with high-risk prostate cancer.

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Key information

Age range

18 year and older

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

Humanitas Clinical and Research Centre & Humanitas University, Rozzano, Milano, Italy

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male patients aged 18 years or older
  • Histologically confirmed unilateral high-risk localized prostate cancer, defined by at least one of the following: ISUP Grade Group 4 or 5; suspicion of at least cT3a disease on multiparametric MRI and/or PSMA PET; or PSA greater than or equal to 20 ng/mL with a unilateral index lesion
  • Unilateral features of the index lesion defined by biopsy, multiparametric MRI, and PSMA PET
  • No PSMA PET-positive pelvic lymph nodes contralateral to the dominant side of the prostate cancer
  • No significant contralateral PSMA uptake on the non-dominant side, defined as lesions with PRIMARY score 3 to 5
  • No contralateral index lesion on multiparametric MRI subsequently confirmed by prostate biopsy
  • No high-risk histology on the side contralateral to the dominant lesion, including ISUP Grade Group greater than 3 or unconventional prostate cancer histology
  • No frank extracapsular invasion or seminal vesicle invasion on the contralateral side
  • Up to two positive systematic cores with unfavorable intermediate-risk disease or up to four with favorable intermediate-risk disease are allowed on the contralateral side
  • A maximum of two pelvic PSMA-positive lymph nodes allowed on the dominant side
  • Clinically localized disease, defined as less than cT4 on multiparametric MRI and no distant metastases, including no retroperitoneal lymph nodes on PSMA PET
  • Life expectancy greater than 10 years according to physician judgment
  • Scheduled for robot-assisted radical prostatectomy and fit for surgery
  • Written informed consent provided

Exclusion criteria

  • Any prostate cancer treatment prior to prostatectomy, including androgen deprivation therapy, neoadjuvant chemotherapy, radiotherapy, or focal ablative therapy
  • Prior active treatment for prostate cancer
  • Contralateral ISUP Grade Group 4 to 5 prostate cancer
  • Contralateral ISUP Grade Group 2 in more than 4 positive cores or ISUP Grade Group 3 in more than 2 positive cores
  • Contralateral cT3 disease on multiparametric MRI
  • N1 or M1 disease on PSMA PET or multiparametric MRI, except for up to two positive pelvic lymph nodes on the dominant side
  • No systematic prostate biopsies performed, with a minimum of 10 cores, and targeted biopsies when a target lesion is present
  • Other active malignancy
  • Contraindication to multiparametric MRI and/or PSMA PET
  • Inability to provide written informed consent
  • Age younger than 18 years
  • ASA score greater than 3
  • Any contraindication to pelvic lymph node dissection
  • Severe psychiatric disease
  • Inadequate hematologic and/or coagulation function
  • Active infection
  • Any other serious medical, psychiatric, psychological, familial, or geographic condition that, in the judgment of the investigator, may interfere with staging, treatment, follow-up, compliance, or increase treatment-related risk
  • Patients with prior malignancy treated with curative intent are eligible only with mandatory approval by the local multidisciplinary tumor board

Treatment and study plan

Unilateral Extended Pelvic Lymph Node Dissection

Procedure

Extended pelvic lymph node dissection performed only on the side of the dominant lesion, as defined by biopsy, multiparametric MRI, and PSMA PET findings.

Bilateral Extended Pelvic Lymph Node Dissection

Procedure

Extended pelvic lymph node dissection performed bilaterally according to the study surgical template during robot-assisted radical prostatectomy.

Primary outcomes

  1. Biochemical Recurrence-Free Survival

    Time frame: 3 years after surgery

    Biochemical recurrence defined as postoperative PSA greater than 0.1 ng/mL with three consecutive rises or initiation of prostate cancer-specific secondary treatment more than 6 months after surgery

  2. PSA Persistence

    Time frame: 8 weeks after surgery

    Postoperative PSA greater than 0.1 ng/mL at 6 weeks after surgery confirmed by an additional PSA measurement performed 2 weeks later.

Secondary outcomes

  1. Perioperative Complications

    Time frame: Up to 6 months after surgery

    Complications graded using the Clavien-Dindo classification and assessed for likelihood of being related to pelvic lymph node dissection.

  2. Operative Time

    Time frame: During surgery

    Total operative time recorded during robot-assisted radical prostatectomy and pelvic lymph node dissection.

  3. Estimated Blood Loss

    Time frame: During surgery

    Intraoperative estimated blood loss.

  4. Length of Hospital Stay

    Time frame: During the index hospitalization, up to 90 days after surgery

    Number of days from surgery to discharge from the index hospitalization.

  5. Overall Prostate Cancer Quality of Life Score Assessed Using the Expanded Prostate Cancer Index Composite for Clinical Practice (EPIC-CP)

    Time frame: 1 year after surgery

    Overall prostate cancer-related quality of life assessed using the Expanded Prostate Cancer Index Composite for Clinical Practice questionnaire. The overall score is calculated by summing the five domain summary scores: urinary incontinence, urinary irritation/obstruction, bowel, sexual, and vitality/hormonal. Total scores range from 0 to 60, with higher scores indicating worse symptoms and poorer quality of life.

  6. Treatment-Free Survival

    Time frame: 3 years after surgery

    Absence of any salvage local or systemic treatment after surgery.

  7. Systemic Treatment-Free Survival

    Time frame: 3 years after surgery

    Absence of systemic treatment after surgery.

  8. Metastasis-Free Survival

    Time frame: 3 years after surgery

    Absence of metastatic disease during follow-up, including PSMA PET assessment when clinically indicated after multidisciplinary discussion.

  9. Cost-Effectiveness

    Time frame: 1 year after surgery

    Cost-effectiveness assessed as incremental cost per quality-adjusted life year at 1 year after surgery.

Study contacts

Contact information is provided by the study sponsor or research team.

Alessandro Marquis, MD

CONTACT

[email protected]

+39 011 633 6591

Chiara Fiameni

CONTACT

[email protected]

+39 011 633 6591

Sponsors and collaborators

Lead sponsor

University of Turin, Italy

Other

Collaborators

  • Associazione Italiana per la Ricerca sul Cancro
  • Fondazione Ricerca Molinette

Registry information

Official study title

Bilateral or Unilateral Extended Pelvic Lymph Node Dissection in High-Risk Prostate Cancer: The BALANCE Randomized Controlled Trial

Acronym: BALANCE

Important dates

Study start
2026
Primary completion
2029
Study completion
2030
First posted
May 12, 2026
Registry last updated
May 12, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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